Functional Significance of Cytochrome P450 1A2 Allelic Variants, P450 1A2*8, *15, and *16 (R456H, P42R, and R377Q)
| Autor: | Hyoung-Goo Park, In-Hyeok Kim, Young-Jin Chun, Songhee Han, Young-Ran Lim, Donghak Kim, Mi-Jung Ko, Chul-Ho Yun |
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| Jazyk: | angličtina |
| Rok vydání: | 2015 |
| Předmět: |
Pharmacology
Nonsynonymous substitution chemistry.chemical_classification Genetics Mutation Wild type CYP1A2 Phenacetin Single-nucleotide polymorphism Biology Methoxyresorufin medicine.disease_cause Biochemistry Enzyme chemistry Drug Discovery medicine Molecular Medicine Original Article Enzyme kinetics Polymorphism Escherichia coli P450 1A2 Allelic variants |
| Zdroj: | Biomolecules & Therapeutics |
| ISSN: | 2005-4483 1976-9148 |
| Popis: | P450 1A2 is responsible for the metabolism of clinically important drugs and the metabolic activation of environmental chemicals. Genetic variations of P450 1A2 can influence its ability to perform these functions, and thus, this study aimed to characterize the functional significance of three P450 1A2 allelic variants containing nonsynonymous single nucleotide polymorphisms (P450 1A2*8, R456H; *15, P42R; *16, R377Q). Variants containing these SNPs were constructed and the recombinant enzymes were expressed and purified in Escherichia coli. Only the P42R variant displayed the typical CO-binding spectrum indicating a P450 holoenzyme with an expression level of ∼ 170 nmol per liter culture, but no P450 spectra were observed for the two other variants. Western blot analysis revealed that the level of expression for the P42R variant was lower than that of the wild type, however the expression of variants R456H and R377Q was not detected. Enzyme kinetic analyses indicated that the P42R mutation in P450 1A2 resulted in significant changes in catalytic activities. The P42R variant displayed an increased catalytic turnover numbers (k cat) in both of methoxyresorufin O-demethylation and phenacetin O-deethylation. In the case of phenacetin O-deethylation analysis, the overall catalytic efficiency (k cat/K m) increased up to 2.5 fold with a slight increase of its K m value. This study indicated that the substitution P42R in the N-terminal proline-rich region of P450 contributed to the improvement of catalytic activity albeit the reduction of P450 structural stability or the decrease of substrate affinity. Characterization of these polymorphisms should be carefully examined in terms of the metabolism of many clinical drugs and environmental chemicals. |
| Databáze: | OpenAIRE |
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